The COQ2 gene homepage

General information
Gene symbol COQ2
Gene name coenzyme Q2 homolog, prenyltransferase (yeast)
Chromosome 4
Chromosomal band q21.23
Imprinted Unknown
Genomic reference NG_015825.1
Transcript reference NM_015697.7
Exon/intron information NM_015697.7 exon/intron table
Associated with diseases COQ10D1, ID, MSA1
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 72
Unique public DNA variants reported 45
Individuals with public variants 11
Hidden variants 8
Notes The establishment of this gene variant database (LSDB) was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement nÂș 200754 - the GEN2PHEN project.
Date created April 05, 2011
Date last updated January 11, 2023
Version COQ2:230111

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_015697.7.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL
HGNC 25223
Entrez Gene 27235
PubMed articles COQ2
OMIM - Gene 609825
OMIM - Diseases COQ10D1 (coenzyme Q10 deficiency, primary, type 1 (COQ10D-1))
MSA1 (multisystem atrophy,, type 1 (MSA-1, Shy-Drager syndrome))
GeneCards COQ2
GeneTests COQ2
Orphanet COQ2

Active transcripts




NCBI ID     

NCBI Protein ID     

00000201 4 coenzyme Q2 homolog, prenyltransferase (yeast) NM_015697.7 NP_056512.5 72

Copyright & disclaimer
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